Evidence map›Paper›PMID 39657158›Full record

ArticleGigaScience2024

Learning a generalized graph transformer for protein function prediction in dissimilar sequences.

Yiwei Fu, Zhonghui Gu, Xiao Luo, Qirui Guo, Luhua Lai, Minghua Deng

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Article in GigaScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
  6. GOBeacon: An ensemble model for protein function prediction enhanced by contrastive learning.Protein science : a publication of the Protein Society · 2025
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yiwei FuSchool of Mathematical Sciences, Peking University, Beijing 100871, China.ORCID 0009-0000-1637-6764
Zhonghui GuPeking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.ORCID 0000-0001-6142-4358
Xiao LuoDepartment of Computer Science, University of California, Los Angeles, CA 90024, USA.ORCID 0000-0002-7987-3714
Qirui GuoCenter for Quantitative Biology, Peking University, Beijing 100871, China.
Luhua LaiPeking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.ORCID 0000-0002-8343-7587
Minghua DengSchool of Mathematical Sciences, Peking University, Beijing 100871, China.ORCID 0000-0002-9143-1898

Funding

National Key Research and Development Program of China 2021YFF1200902National Natural Science Foundation of China 32270689
6 · The paper itself

Abstract

backgroundIn the face of a growing disparity between high-throughput sequence data and low-throughput experimental studies, the emerging field of deep learning stands as a promising alternative. Generally, many data-driven approaches are capable of facilitating fast and accurate predictions of protein functions. Nevertheless, the inherent statistical nature of deep learning techniques may limit their generalization capabilities when applied to novel nonhomologous proteins that diverge significantly from existing ones.

resultsIn this work, we herein propose a novel, generalized approach named Graph Adversarial Learning with Alignment (GALA) for protein function prediction. Our GALA method integrates a graph transformer architecture with an attention pooling module to extract embeddings from both protein sequences and structures, facilitating unified learning of protein representations. Particularly noteworthy, GALA incorporates a domain discriminator conditioned on both learnable representations and predicted probabilities, which undergoes adversarial learning to ensure representation invariance across diverse environments. To optimize the model with abundant label information, we generate label embeddings in the hidden space, explicitly aligning them with protein representations. Benchmarked on datasets derived from the PDB database and Swiss-Prot database, our GALA achieves considerable performance comparable to several state-of-the-art methods. Even more, GALA demonstrates wonderful biological interpretability by identifying significant functional residues associated with Gene Ontology terms through class activation mapping.

conclusionsGALA, which leverages adversarial learning and label embedding alignment to acquire domain-invariant protein representations, exhibits outstanding generalizability in function prediction for proteins from previously unseen sequence space. By incorporating the structures predicted by AlphaFold2, GALA demonstrates significant potential for function annotation in newly discovered sequences. A detailed implementation of our GALA is available at https://github.com/fuyw-aisw/GALA.

Indexed as

ProteinsAlgorithmsComputational BiologyDatabases, ProteinDeep LearningSequence Analysis, ProteinProteinsadversarial learningdomain adaptationgraph transformerlow sequence identityprotein function prediction

Identifiers

PMID39657158
PMCPMC11734293

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.